A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431206



Internal ID22489076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47060170..47060237hg38UCSC Ensembl
chr6:47027906..47027973hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898020
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431206
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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